Overview

> project_summary = "/Users/rory/cache/fabio-splicing/new-samples/2016-07-29_fabio-newlines/project-summary.csv"
> counts_file = "/Users/rory/cache/fabio-splicing/new-samples/2016-07-29_fabio-newlines/combined.counts"
> tx2genes_file = "/Users/rory/cache/fabio-splicing/new-samples/2016-07-29_fabio-newlines/tx2gene.csv"
> cbPalette <- c("#999999", "#E69F00", "#56B4E9", "#009E73", "#F0E442", "#0072B2", 
+     "#D55E00", "#CC79A7")
> summarydata = read.table(project_summary, header = TRUE, sep = ",")
> summarydata = summarydata[, colSums(is.na(summarydata)) < nrow(summarydata)]
> # handle newer bcbio-nextgen runs that use description as the key
> if ("description" %in% colnames(summarydata)) {
+     rownames(summarydata) = summarydata$description
+     summarydata$Name = rownames(summarydata)
+     summarydata$description = NULL
+ } else {
+     rownames(summarydata) = summarydata$Name
+     # summarydata$Name = NULL
+ }
> summarydata = summarydata[order(rownames(summarydata)), ]
> if (file.exists(tx2genes_file)) {
+     sample_dirs = file.path(dirname(project_summary), "..", rownames(summarydata))
+     salmon_files = file.path(sample_dirs, "salmon", "quant.sf")
+     sailfish_files = file.path(sample_dirs, "sailfish", "quant.sf")
+     new_sailfish = file.path(sample_dirs, "sailfish", "quant", "quant.sf")
+     new_salmon = file.path(sample_dirs, "salmon", "quant", "quant.sf")
+     if (file.exists(salmon_files[1])) {
+         sf_files = salmon_files
+     } else if (file.exists(sailfish_files[1])) {
+         sf_files = sailfish_files
+     } else if (file.exists(new_sailfish[1])) {
+         sf_files = new_sailfish
+     } else if (file.exists(new_salmon[1])) {
+         sf_files = new_salmon
+     }
+     names(sf_files) = rownames(summarydata)
+     tx2gene = read.table(tx2genes_file, sep = ",", row.names = NULL, header = FALSE)
+     txi.salmon = tximport(sf_files, type = "salmon", tx2gene = tx2gene, reader = readr::read_tsv, 
+         countsFromAbundance = "lengthScaledTPM")
+     counts = round(data.frame(txi.salmon$counts, check.names = FALSE))
+ } else {
+     counts = read.table(counts_file, header = TRUE, row.names = "id", check.names = FALSE)
+ }
> counts = counts[, order(colnames(counts)), drop = FALSE]
> colnames(counts) = gsub(".counts", "", colnames(counts))
> 
> # this is a list of all non user-supplied metadata columns that could appear
> known_columns = c("Name", "X.GC", "Exonic.Rate", "Sequences.flagged.as.poor.quality", 
+     "rRNA_rate", "Fragment.Length.Mean", "Intronic.Rate", "Intergenic.Rate", 
+     "Mapping.Rate", "Quality.format", "Duplication.Rate.of.Mapped", "Mapped", 
+     "rRNA", "Sequence.length", "Transcripts.Detected", "Mean.Per.Base.Cov.", 
+     "Genes.Detected", "Unique.Starts.Per.Read", "unique_starts_per_read", "complexity", 
+     "X5.3.bias", "Duplicates.pct", "Duplicates", "Mapped.reads", "Average.insert.size", 
+     "Mapped.reads.pct", "Total.reads", "avg_coverage_per_region", "Mapped.Reads")
> summarydata[, "Fragment.Length.Mean"] = summarydata$Average.insert.size
> metadata = summarydata[, !colnames(summarydata) %in% known_columns, drop = FALSE]
> metadata = metadata[, colSums(is.na(metadata)) < nrow(metadata), drop = FALSE]
> metadata$treatment = relevel(metadata$treatment, ref = "Ctrl")
> metadata$bort = relevel(metadata$bort, ref = "N")
> metadata$e7107 = relevel(metadata$e7107, ref = "N")

> mart <- biomaRt::useMart(biomart = "ensembl", dataset = "hsapiens_gene_ensembl")
> t2g <- biomaRt::getBM(attributes = c("ensembl_transcript_id", "ensembl_gene_id", 
+     "external_gene_name", "gene_biotype", "transcript_biotype"), mart = mart)
> t2g <- dplyr::rename(t2g, target_id = ensembl_transcript_id, ens_gene = ensembl_gene_id, 
+     ext_gene = external_gene_name)
> symbols = unique(t2g[, c("ens_gene", "ext_gene", "gene_biotype")])

> sanitize_datatable = function(df, ...) {
+     # remove dashes which cause wrapping
+     DT::datatable(df, ..., rownames = gsub("-", "_", rownames(df)), colnames = gsub("-", 
+         "_", colnames(df)))
+ }

> # set seed for reproducibility
> set.seed(1454944673)

Sample metadata

> get_heatmap_fn = function(summarydata) {
+     # return the pheatmap function with or without metadata
+     if (ncol(metadata) == 0) {
+         return(pheatmap)
+     } else {
+         # rownames(metadata) = summarydata$Name
+         heatmap_fn = function(data, ...) {
+             pheatmap(data, annotation = metadata, clustering_method = "ward.D2", 
+                 clustering_distance_cols = "correlation", ...)
+         }
+         return(heatmap_fn)
+     }
+ }
> heatmap_fn = get_heatmap_fn(summarydata)

Quality control metrics

> qualimap_run = "Mapped" %in% colnames(summarydata)
> do_quality = "Mapped.reads" %in% colnames(summarydata)

Mapped reads

Overall mapped reads looks good.

> ggplot(summarydata, aes(x = Name, y = Mapped)) + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     geom_bar(stat = "identity") + ylab("mapped reads") + xlab("")

> ggplot(summarydata, aes(x = Name, y = Mapped.reads)) + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     geom_bar(stat = "identity") + ylab("mapped reads") + xlab("")

Genomic mapping rate

Genomic mapping rate looks great.

> ggplot(summarydata, aes(x = Name, y = Mapping.Rate)) + geom_bar(stat = "identity") + 
+     ylab("mapping rate") + xlab("") + theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90))

> ggplot(summarydata, aes(x = Name, y = Mapped.reads.pct)) + geom_bar(stat = "identity") + 
+     ylab("mapping rate") + xlab("") + theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90))

Number of genes detected

Good number of genes detected.

> dd = data.frame(Name = colnames(counts), Genes.Detected = colSums(counts > 0))
> ggplot(dd, aes(x = Name, y = Genes.Detected)) + geom_bar(stat = "identity") + 
+     theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90)) + ylab("genes detected") + 
+     xlab("")

Gene detection saturation

This plot looks a little off, but it is the way the axis are. It is fine.

> col_mapped = ifelse(qualimap_run, "Mapped", "Mapped.reads")
> dd = data.frame(Mapped = summarydata[, col_mapped], Genes.Detected = colSums(counts > 
+     0))
> ggplot(dd, aes(x = Mapped, y = Genes.Detected)) + geom_point() + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     ylab("genes detected") + xlab("reads mapped")

Exonic mapping rate

Here we are starting to see some issues that might be batch effects. Ctrl and Bort1 samples have slightly higher exonic mapping rate.

> ggplot(summarydata, aes(x = Name, y = Exonic.Rate)) + geom_bar(stat = "identity") + 
+     theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90)) + ylab("exonic mapping rate") + 
+     xlab("")

rRNA mapping rate

They also have a lower rRNA rate:

> eval_rRNA = "rRNA_rate" %in% colnames(summarydata) & !sum(is.na(summarydata$rRNA_rate)) == 
+     nrow(summarydata)

> ggplot(summarydata, aes(x = Name, y = rRNA_rate)) + geom_bar(stat = "identity") + 
+     theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90)) + ylab("rRNA rate") + 
+     xlab("")

Estimated fragment length of paired-end reads

and a higher estimated fragment size

> ggplot(summarydata, aes(x = Name, y = Fragment.Length.Mean)) + geom_bar(stat = "identity") + 
+     theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90)) + ylab("fragment length") + 
+     xlab("")

5’->3’ bias

> ggplot(summarydata, aes(x = Name, y = X5.3.bias)) + geom_bar(stat = "identity") + 
+     theme_bw(base_size = 10) + theme(panel.grid.major = element_line(size = 0.5, 
+     color = "grey"), axis.text.x = element_text(angle = 90)) + ylab("5'->3' bias") + 
+     xlab("")

Boxplot of log10 counts per gene

> melted = melt(counts)
> colnames(melted) = c("sample", "count")
> melted$sample = factor(melted$sample)
> melted = melted[order(melted$sample), ]
> melted$count = log(melted$count)
> ggplot(melted, aes(x = sample, y = count)) + geom_boxplot() + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     xlab("")

Boxplot of log10 TMM-normalized counts per gene

Trimmed mean of M-values (TMM) normalization is described here

Robinson, M. D., & Oshlack, A. (2010). A scaling normalization method for differential expression analysis of RNA-seq data. Genome Biology, 11(3). doi:10.1186/gb-2010-11-3-r25

> y = DGEList(counts = counts)
> y = calcNormFactors(y)
> normalized_counts = cpm(y, normalized.lib.sizes = TRUE)
> melted = melt(normalized_counts)
> colnames(melted) = c("gene", "sample", "count")
> melted$sample = factor(melted$sample)
> melted = melted[order(melted$sample), ]
> melted$count = log(melted$count)
> ggplot(melted, aes(x = sample, y = count)) + geom_boxplot() + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     xlab("")

Density of log10 TMM-normalized counts

> ggplot(melted, aes(x = count, group = sample)) + geom_density() + theme_bw(base_size = 10) + 
+     theme(panel.grid.major = element_line(size = 0.5, color = "grey"), axis.text.x = element_text(angle = 90)) + 
+     xlab("")

Correlation heatmap of TMM-normalized counts

The control and bort samples are more similar to each other than the other samples. We won’t be able to tell if that is due to real differences or some of the batch differences we saw above.

Correlation (Pearson)

> heatmap_fn(cor(normalized_counts, method = "pearson"))

Correlation (Spearman)

> heatmap_fn(cor(normalized_counts, method = "spearman"))

PCA plots

We can see the same effects on the PCA plot. The different treatments separate out the cells, bort + control are more similar to each other and E7107 + BE are more similar to each other. It looks like the E7107 treatment is the strongest effect as most of the variance is explained by whether or not the samples have been treated with E7107.

> dds = DESeqDataSetFromMatrix(countData = counts, colData = summarydata, design = ~Name)
> vst = varianceStabilizingTransformation(dds)
> pca_loadings = function(object, ntop = 500) {
+     rv <- matrixStats::rowVars(assay(object))
+     select <- order(rv, decreasing = TRUE)[seq_len(min(ntop, length(rv)))]
+     pca <- prcomp(t(assay(object)[select, ]))
+     percentVar <- pca$sdev^2/sum(pca$sdev^2)
+     names(percentVar) = colnames(pca$x)
+     pca$percentVar = percentVar
+     return(pca)
+ }
> pc = pca_loadings(vst)
> comps = data.frame(pc$x)
> comps$Name = rownames(comps)
> library(dplyr)
> comps = comps %>% left_join(summarydata, by = c(Name = "Name"))
> colorby = "treatment"

> pca_plot = function(comps, nc1, nc2, colorby) {
+     c1str = paste0("PC", nc1)
+     c2str = paste0("PC", nc2)
+     ggplot(comps, aes_string(c1str, c2str, color = colorby)) + geom_point() + 
+         theme_bw() + xlab(paste0(c1str, ": ", round(pc$percentVar[nc1] * 100), 
+         "% variance")) + ylab(paste0(c2str, ": ", round(pc$percentVar[nc2] * 
+         100), "% variance"))
+ }

PC1 vs. PC2

> pca_plot(comps, 1, 2, colorby)

PC3 vs. PC4

> pca_plot(comps, 3, 4, colorby)

PC5 vs. PC6

> pca_plot(comps, 5, 6, colorby)

Variance explained by component

> ggplot(data.frame(component = reorder(names(pc$percentVar), -pc$percentVar), 
+     percent_var = pc$percentVar), aes(component, percent_var)) + geom_bar(stat = "identity") + 
+     ylab("percent of total variation") + xlab("") + theme_bw()

> # snagged from development version of DESeq
> DESeqDataSetFromTximport <- function(txi, colData, design, ...) {
+     counts <- round(txi$counts)
+     mode(counts) <- "integer"
+     dds <- DESeqDataSetFromMatrix(countData = counts, colData = colData, design = design, 
+         ...)
+     stopifnot(txi$countsFromAbundance %in% c("no", "scaledTPM", "lengthScaledTPM"))
+     if (txi$countsFromAbundance %in% c("scaledTPM", "lengthScaledTPM")) {
+         message("using length scaled TPM counts from tximport")
+     } else {
+         message("using counts and average transcript lengths from tximport")
+         lengths <- txi$length
+         dimnames(lengths) <- dimnames(dds)
+         assays(dds)[["avgTxLength"]] <- lengths
+     }
+     return(dds)
+ }
> 
> subset_tximport = function(txi, rows, columns) {
+     txi$counts = txi$counts[rows, columns]
+     txi$abundance = txi$abundance[rows, columns]
+     txi$length = txi$length[rows, columns]
+     return(txi)
+ }

> library(DEGreport)
> library(vsn)
> design = ~treatment
> condition = "treatment"

Differential expression

> counts <- counts[rowSums(counts > 0) > 1, ]
> if (exists("txi.salmon")) {
+     txi.salmon = subset_tximport(txi.salmon, rownames(counts), colnames(counts))
+     dds = DESeqDataSetFromTximport(txi.salmon, colData = summarydata, design = design)
+ } else {
+     dds = DESeqDataSetFromMatrix(countData = counts, colData = summarydata, 
+         design = design)
+ }
> geoMeans = apply(counts, 1, function(row) if (all(row == 0)) 0 else exp(mean(log(row[row != 
+     0]))))
> dds = estimateSizeFactors(dds, geoMeans = geoMeans)
> dds = DESeq(dds)

Effect of variance stabilization

> par(mfrow = c(1, 3))
> notAllZero <- (rowSums(counts(dds)) > 0)
> rld <- rlog(dds)
> vsd <- varianceStabilizingTransformation(dds)
> rlogMat <- assay(rld)
> vstMat <- assay(vsd)
> 
> meanSdPlot(log2(counts(dds, normalized = TRUE)[notAllZero, ] + 1))

> meanSdPlot(assay(rld[notAllZero, ]))

> meanSdPlot(assay(vsd[notAllZero, ]))

Dispersion estimates

The dispersion estimates are super low, I guess because it is cell lines? Just to be clear, these are biological replicates right? Different replicates of the same treatment were done on different days to different batches?

replicates;

> plotDispEsts(dds)

> e7107 = results(dds, contrast = c("treatment", "E7107", "Ctrl"))
> bort = results(dds, contrast = c("treatment", "Bort", "Ctrl"))
> be = results(dds, contrast = c("treatment", "BE", "Ctrl"))
> plotMA_full = function(res) {
+     ymax = max(res$log2FoldChange, na.rm = TRUE)
+     ymin = min(res$log2FoldChange, na.rm = TRUE)
+     plotMA(res, ylim = c(ymin, ymax))
+ }
> volcano = function(res) {
+     stats = as.data.frame(res[, c(2, 6)])
+     p = volcano_density_plot(stats, lfc.cutoff = 1.5)
+     print(p)
+ }
> write_deseq = function(res, fname) {
+     out_df = as.data.frame(res)
+     out_df$id = rownames(out_df)
+     out_df = out_df[, c("id", colnames(out_df)[colnames(out_df) != "id"])]
+     out_df = out_df %>% left_join(symbols, by = c(id = "ens_gene")) %>% arrange(padj)
+     write.table(out_df, file = fname, quote = FALSE, sep = ",", row.names = FALSE, 
+         col.names = TRUE)
+ }

Bort vs control

> plotMA_full(bort)

> volcano(bort)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                grob
1 1 (2-2,1-1) arrange     gtable[arrange]
2 2 (2-2,2-2) arrange     gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.178]

> write_deseq(bort, "control-vs-bort-deseq2.csv")

E7107 vs control

> plotMA_full(e7107)

> volcano(e7107)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                grob
1 1 (2-2,1-1) arrange     gtable[arrange]
2 2 (2-2,2-2) arrange     gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.346]

> write_deseq(e7107, "control-vs-e7107-deseq2.csv")

BE vs control

> plotMA_full(be)

> volcano(be)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                grob
1 1 (2-2,1-1) arrange     gtable[arrange]
2 2 (2-2,2-2) arrange     gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.514]

> write_deseq(be, "control-vs-be-deseq2.csv")

sleuth

> library(dplyr)
> library(sleuth)
> sf_dirs = file.path("..", "..", rownames(summarydata), "sailfish", "quant")
> names(sf_dirs) = rownames(summarydata)
> sfdata = metadata
> sfdata$sample = rownames(sfdata)
> sfdata$path = sf_dirs
> mart <- biomaRt::useMart(biomart = "ensembl", dataset = "hsapiens_gene_ensembl")
> t2g <- biomaRt::getBM(attributes = c("ensembl_transcript_id", "ensembl_gene_id", 
+     "external_gene_name", "gene_biotype", "transcript_biotype"), mart = mart)
> t2g <- dplyr::rename(t2g, target_id = ensembl_transcript_id, ens_gene = ensembl_gene_id, 
+     ext_gene = external_gene_name)

Control vs BE

> library(biomaRt)
> so = sleuth_prep(sfdata, design, target_mapping = t2g) %>% sleuth_fit()
> models(so)
> save(so, file = "sleuth_models.RData")
> rm(so)

> load("sleuth_models.RData")
> so = sleuth_wt(so, "treatmentBE")
> so = sleuth_wt(so, "treatmentBort")
> so = sleuth_wt(so, "treatmentE7107")
> bort_tab = sleuth_results(so, "treatmentBort", show_all = TRUE)
> e7107_tab = sleuth_results(so, "treatmentE7107", show_all = TRUE)
> be_tab = sleuth_results(so, "treatmentBE", show_all = TRUE)

> reciprocal_sleuth = function(tab) {
+     tab %>% na.omit() %>% group_by(ens_gene) %>% mutate(reciprocal = (sum(b > 
+         0 & qval < 0.05) > 0) & sum(b < 0 & qval < 0.05) > 0 & length(ens_gene) > 
+         1) %>% as.data.frame()
+ }
> bort_tab = reciprocal_sleuth(bort_tab)
> e7107_tab = reciprocal_sleuth(e7107_tab)
> be_tab = reciprocal_sleuth(be_tab)
> write.table(bort_tab, "control-vs-bort-sleuth.csv", quote = FALSE, row.names = FALSE, 
+     col.names = TRUE, sep = ",")
> write.table(e7107_tab, "control-vs-e7107-sleuth.csv", quote = FALSE, row.names = FALSE, 
+     col.names = TRUE, sep = ",")
> write.table(be_tab, "control-vs-be-sleuth.csv", quote = FALSE, row.names = FALSE, 
+     col.names = TRUE, sep = ",")

Transcript MA plots

> library(cowplot)
> sleuth_MA = function(results) {
+     results$DE = results$qval < 0.05
+     ggplot(results, aes(mean_obs, b, color = DE)) + geom_point(size = 0.5) + 
+         guides(color = FALSE) + scale_color_manual(values = c("black", "red")) + 
+         xlab("mean expression") + ylab(expression("<U+0392>")) + scale_x_log10()
+ }

Control vs Bort

> sleuth_MA(bort_tab)

Control vs E7107

> sleuth_MA(e7107_tab)

Control vs BE

> sleuth_MA(be_tab)

Pathway analysis

> orgdb = "org.Hs.eg.db"
> biomart_dataset = "hsapiens_gene_ensembl"
> keggname = "hsa"
> library(dplyr)
> library(clusterProfiler)
> library(orgdb, character.only = TRUE)
> library(biomaRt)

> mart = biomaRt::useMart(biomart = "ensembl", dataset = biomart_dataset)
> entrez = biomaRt::getBM(attributes = c("ensembl_gene_id", "entrezgene"), mart = mart)
> entrez$entrezgene = as.character(entrez$entrezgene)

> summarize_cp = function(res, comparison) {
+     summaries = data.frame()
+     for (ont in names(res)) {
+         ontsum = summary(res[[ont]])
+         ontsum$ont = ont
+         summaries = rbind(summaries, ontsum)
+     }
+     summaries$comparison = comparison
+     summaries = summaries %>% arrange(qvalue)
+     return(summaries)
+ }
> 
> enrich_cp = function(res, comparison) {
+     res = data.frame(res)
+     res = res %>% tibble::rownames_to_column() %>% left_join(entrez, by = c(rowname = "ensembl_gene_id")) %>% 
+         filter(!is.na(entrezgene))
+     universe = res$entrezgene
+     genes = subset(res, padj < 0.05)$entrezgene
+     mf = enrichGO(genes, universe = universe, OrgDb = orgdb, ont = "MF", pAdjustMethod = "BH", 
+         qvalueCutoff = 1, pvalueCutoff = 1)
+     cc = enrichGO(genes, universe = universe, OrgDb = orgdb, ont = "CC", pAdjustMethod = "BH", 
+         qvalueCutoff = 1, pvalueCutoff = 1)
+     bp = enrichGO(genes, universe = universe, OrgDb = orgdb, ont = "BP", pAdjustMethod = "BH", 
+         qvalueCutoff = 1, pvalueCutoff = 1)
+     kg = enrichKEGG(gene = genes, universe = universe, organism = "hsa", pvalueCutoff = 1, 
+         qvalueCutoff = 1, pAdjustMethod = "BH")
+     all = list(mf = mf, cc = cc, bp = bp, kg = kg)
+     all[["summary"]] = summarize_cp(all, comparison)
+     return(all)
+ }

> gsea_cp = function(res, comparison) {
+     res = res %>% data.frame() %>% tribble::rownames_to_column() %>% left_join(entrez, 
+         by = c(rowname = "ensembl_gene_id")) %>% filter(!is.na(entrezgene)) %>% 
+         filter(!is.na(log2FoldChange)) %>% filter(!is.na(lfcSE))
+     lfc = data.frame(res)[, "log2FoldChange"]
+     lfcse = data.frame(res)[, "lfcSE"]
+     genes = lfc/lfcse
+     names(genes) = res$entrezgene
+     genes = genes[order(genes, decreasing = TRUE)]
+     cc = gseGO(genes, ont = "CC", OrgDb = orgdb, nPerm = 500, pvalueCutoff = 1, 
+         pAdjustMethod = "BH", verbose = TRUE)
+     mf = gseGO(genes, ont = "MF", OrgDb = orgdb, nPerm = 500, pvalueCutoff = 1, 
+         pAdjustMethod = "BH", verbose = TRUE)
+     bp = gseGO(genes, ont = "bp", OrgDb = orgdb, nPerm = 500, pvalueCutoff = 1, 
+         pAdjustMethod = "BH", verbose = TRUE)
+     genes = data.frame(res)[, "log2FoldChange"]
+     names(genes) = res$entrezgene
+     genes = genes[order(genes, decreasing = TRUE)]
+     genes = genes[!is.na(genes)]
+     kg = gseKEGG(geneList = genes, organism = "mmu", nPerm = 500, pvalueCutoff = 1, 
+         verbose = TRUE)
+     if (orgdb == "org.Hs.eg.db") {
+         do = summary(gseDO(geneList = genes, nPerm = 500, pvalueCutoff = 1, 
+             pAdjustMethod = "BH", verbose = TRUE))
+         do$ont = "DO"
+         all = list(mf = mf, cc = cc, bp = bp, kg = kg, do = do)
+     } else {
+         all = list(mf = mf, cc = cc, bp = bp, kg = kg)
+     }
+     all[["summary"]] = summarize_cp(all, comparison)
+     return(all)
+ }
> write_enrich = function(res, filename) {
+     res = subset(res, qvalue < 0.05)
+     write.table(res, file = filename, quote = FALSE, sep = ",", row.names = FALSE, 
+         col.names = TRUE)
+ }

Enriched pathways

Here we take the set of genes that are flagged as significantly different for each comparison and look for pathways that tend to be enriched for these genes.

Bort vs control

> bort_enrich = enrich_cp(bort, "Bort")
> write_enrich(bort_enrich$summary, "control-bort-pathway.csv")

E7107 vs control

> e7107_enrich = enrich_cp(e7107, "e7107")
> write_enrich(e7107_enrich$summary, "control-e7107-pathway.csv")

BE vs control

> be_enrich = enrich_cp(be, "BE")
> write_enrich(be_enrich$summary, "control-be-pathway.csv")

TPM matrix

> tpm = so$obs_norm %>% dplyr::select(target_id, sample, tpm) %>% tidyr::spread(sample, 
+     tpm)
> library(biomaRt)
> library(dplyr)
> human = useMart(biomart = "ENSEMBL_MART_ENSEMBL", dataset = "hsapiens_gene_ensembl", 
+     host = "jul2015.archive.ensembl.org")
> symbols = getBM(attributes = c("ensembl_transcript_id", "external_gene_name", 
+     "gene_biotype", "transcript_biotype"), mart = human)
> tpm = tpm %>% left_join(symbols, by = c(target_id = "ensembl_transcript_id"))
> write.table(tpm, file = "tpm.csv", quote = FALSE, col.names = TRUE, row.names = FALSE, 
+     sep = ",")

DE tables

Bort vs ctrl

BE vs ctrl

E7107 vs ctrl

Control vs bort

Control vs be

Control vs e7017

Pathway tables

Description of these tables:

GeneRatio = (# genes in this set DE) / (total genes DE)
BgRatio = (# genes expressed in this set) / (total genes expressed)
geneID = Entrez IDs of genes that are DE in this set
ont = ontological term tested (MF=molecular function, CC=cellular compartment,
 BP=biological process, KG=KEGG pathway)

Control vs bort

Control vs e7107

Control vs BE

TPM matrix

TPM matrix

Treatment interactions

When we did the pairwise comparisons, it made it hard to answer questions about what the effect of treating with both Bortezomib and E7107 is, without resorting to a crappy solution of doing Venn diagrams of the DE genes.

To get at that question, we’ll look at the data slightly differently, instead of comparing the treated back to the control samples, we instead are going to look for effects that are specific to the treatment with Bortezomib or E7107 alone and also look for genes that are specifically turned on when both are treated. To do that we will re-analyze the data, but fit a model with an interaction term, and then test for the effects of treatment with Bort alone, treatment with E7107 alone and treamtent with both Bort and E7107.

> summarydata$bort = ifelse(summarydata$treatment == "Bort", "yes", ifelse(summarydata$treatment == 
+     "BE", "yes", "no"))
> summarydata$E7107 = ifelse(summarydata$treatment == "E7107", "yes", ifelse(summarydata$treatment == 
+     "BE", "yes", "no"))
> design = ~bort + E7107 + bort:E7107
> if (exists("txi.salmon")) {
+     txi.salmon = subset_tximport(txi.salmon, rownames(counts), colnames(counts))
+     dds = DESeqDataSetFromTximport(txi.salmon, colData = summarydata, design = design)
+ } else {
+     dds = DESeqDataSetFromMatrix(countData = counts, colData = summarydata, 
+         design = design)
+ }
> geoMeans = apply(counts, 1, function(row) if (all(row == 0)) 0 else exp(mean(log(row[row != 
+     0]))))
> dds = estimateSizeFactors(dds, geoMeans = geoMeans)
> dds = DESeq(dds)
> symbols = unique(t2g[, c("ens_gene", "ext_gene", "gene_biotype")])

Bort effect

> bort = results(dds, name = "bort_yes_vs_no")
> plotMA_full(bort)

> volcano(bort)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                 grob
1 1 (2-2,1-1) arrange      gtable[arrange]
2 2 (2-2,2-2) arrange      gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.1018]

> write_deseq(bort, "bort-effect.csv")

E7107 effect

> e7107 = results(dds, name = "E7107_yes_vs_no")
> plotMA_full(e7107)

> volcano(e7107)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                 grob
1 1 (2-2,1-1) arrange      gtable[arrange]
2 2 (2-2,2-2) arrange      gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.1186]

> write_deseq(e7107, "E7107-effect.csv")

Combined treatment effect

> combined = results(dds, name = "bortyes.E7107yes")
> plotMA_full(combined)

> volcano(combined)

TableGrob (2 x 2) "arrange": 3 grobs
  z     cells    name                 grob
1 1 (2-2,1-1) arrange      gtable[arrange]
2 2 (2-2,2-2) arrange      gtable[arrange]
3 3 (1-1,1-2) arrange text[GRID.text.1354]

> write_deseq(combined, "combined-effect.csv")

Technical replicates?

These samples are all very very similar to each other within a sample class, you can see they are almost perfectly correlated using Pearson correlation:

> library(corrplot)
> m = cor(counts)
> corrplot(m, method = "number")

Effect tables

Bort effect

E7107 effect

Combined effect

I talked with Praveen and it sounded like these were closer to being technical variants than biological variants in terms of the experimental setup, and the extremely high degree of correlation supports that. If that is true, it might be worthwhile to just look at one sample of each and pretend like the experiment was run with no replicates. We’re in kind of a tough spot because treating technical replicates as biological replicates is wrong, and leads to what we are seeing where there are very high confidence changes when there is only a small difference. If we do it the other way with no replicates, then we lose a lot of power. However if these are actually technical replicates than the ‘power’ we have is illusory since it isn’t based on anything real.